138372-38-0

Upstream product

• 89137-25-7 (S)-2-((S)-2-{2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-acetylamino}-3-phenyl-propionylamino)-4-methyl-pentanoic acid tert-butyl ester 
• 28635-78-1 L-phenylalanyl-L-leucine tert-butyl ester 
• 2748-02-9 L-leucine tert-butyl ester hydrochloride 
• 35661-40-6 N-Fmoc L-Phe 
• 29022-11-5 N-(fluoren-9-ylmethoxycarbonyl)glycine 
• 71989-38-3 Fmoc-Tyr(tBu)-OH 
• 760-84-9 L-leucine hydrochloride 
• 77426-98-3 Gly-Gly-Phe-Leu-OBu^t 
• 139448-95-6 Fmoc-Tyr(Bu^t)-SH 
• 149204-99-9 Fmoc-Gly-L-Phe-L-Leu-OtBu 
• 84891-01-0 Fmoc-Phe-Leu-OtBu 
• 82362-19-4 Gly-Phe-Leu(t-Bu) 

Downstream Products

• 81678-16-2 leucine enkephalin acetate 
• 427881-22-9 (S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-tert-butoxy-phenyl)-propionylamino]-acetylamino}-acetylamino)-3-phenyl-propionylamino]-4-methyl-pentanoic acid tert-butyl ester 

Relevant academic research and scientific papers

Carbocations in action. Design, synthesis, and evaluation of a highly acid-sensitive naphthalene-based backbone amide linker for solid-phase synthesis

(Diagram presented) The design, synthesis, and properties of an extremely acid-labile backbone amide linker based on a regiospecifically substituted tetraalkoxy naphthaldehyde core are presented. This handle enables cleavage of peptide backbone amides (se

A new method for rapid solution synthesis of shorter peptides by use of PyBOP

By using PyBOP promoted coupling of Fmoc protected amino acids, and adopting the deprotection/washing procedure of the Fmoc Amino Acid Chloride Solution Technique (FAACST), a sample of [leucine5] enkephalin has been synthesized in a rapid, cont

Formation of Peptide Thioamides by Use of Fmoc Amino Monothioacids and by PyBOP

Endothiopeptides have been obtained by using PyBOP promoted coupling between Fmoc-protected amino monothioacids and amino acid or peptide esters.The protected endothiopeptides (Fmoc-Gly-Φ(CSNH)-Phe-OEt, Fmoc-Tyr(But)-Φ(CSNH)-Gly-Gly-Phe-Leu-